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rs267608427

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs267608427(-;-)
Make rs267608427(-;A)
Make rs267608427(A;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position154032466
GeneMECP2
is asnp
is mentioned by
dbSNPrs267608427
ebirs267608427
HLIrs267608427
Exacrs267608427
Varsomers267608427
Maprs267608427
PheGenIrs267608427
hapmaprs267608427
1000 genomesrs267608427
hgdprs267608427
ensemblrs267608427
gopubmedrs267608427
geneviewrs267608427
scholarrs267608427
googlers267608427
pharmgkbrs267608427
gwascentralrs267608427
openSNPrs267608427
23andMers267608427
23andMe allrs267608427
SNP Nexus

SNPshotrs267608427
SNPdbers267608427
MSV3drs267608427
GWAS Ctlgrs267608427
Max Magnitude0
ClinVar
Risk rs267608427(A;A)
Alt rs267608427(A;A)
Reference rs267608427(;)
Significance Pathogenic
Disease Rett syndrome
Variation info
Gene MECP2
CLNDBN Rett syndrome
Reversed 1
HGVS NC_000023.10:g.153297918dupT
CLNSRC
CLNACC RCV000132946.2,